• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services


  • Print
  • Share
  • E-mail

Midol Extended Relief (220 mg naproxen sodium) caplet [OTC]

Label is not available on Drugs@FDA

Detailed View: Safety Labeling Changes Approved By FDA Center for Drug Evaluation and Research (CDER) -- April 2009


The detailed view includes drug products with safety labeling changes to the BOXED WARNING, CONTRAINDICATIONS, WARNINGS, PRECAUTIONS, ADVERSE REACTIONS, or PATIENT PACKAGE INSERT/MEDICATION GUIDE sections. Deletions or editorial revisions made to these sections are not included in this summary. Read about the new physician labeling format.

Summary View


Sections Modified

Summary of Changes to Contraindications and Warnings



  • Revised cardiovascular warning
    • "When using this product the risk of heart attack or stroke may increase if you use more than directed or for longer than directed"
  • Addition of the warning statement
    • "Ask a doctor before use if you have asthma